GMP Documentation Specialist (Coordinator I)

A biopharmaceutical company is seeking a Document Control Coordinator I/II in Durham, North Carolina. This role involves the meticulous review, control, and archival of cGMP documentation supporting regulated manufacturing and quality operations. Candidates should have relevant experience and skills in document management and a strong attention to detail. Both Coordinator I and II levels are open, depending on experience. This position offers opportunities to contribute to regulatory inspections and audits. #J-18808-Ljbffr